TREANDA is a uniquely designed agent

TREANDA may cause dual cell death via multiple pathways1-4

TREANDA MoA
Adapted with permission from Oncology NEWS International.

TREANDA is active against both quiescent and dividing cells

  • The exact mechanism of action of TREANDA remains unknown

Bendamustine has been used in over 67,000 patients in the US and Europe since 19945

TREANDA has a novel dual structure

TREANDA structure

TREANDA was synthesized as a unique chemical structure combining an alkylating group with a purine-like benzimidazole ring in 19635

  • The alkylating group contains mechlorethamine, which confers alkylating properties
  • The benzimidazole component contains a purine-like benzimidazole ring

Indications

TREANDA is indicated for the treatment of patients with chronic lymphocytic leukemia (CLL). Efficacy relative to first-line therapies other than chlorambucil has not been established.

TREANDA is indicated for the treatment of patients with indolent B-cell non-Hodgkin’s lymphoma (NHL) that has progressed during or within 6 months of treatment with rituximab or a rituximab-containing regimen.

Important Safety Information

  • Serious adverse reactions, including myelosuppression, infections, infusion reactions and anaphylaxis, tumor lysis syndrome, skin reactions including SJS/TEN, other malignancies, and extravasation, have been associated with TREANDA. Some reactions, such as myelosuppression, infections, and SJS/TEN (when TREANDA was administered concomitantly with allopurinol and other medications known to cause SJS/TEN), have been fatal. Patients should be monitored closely for these reactions and treated promptly if any occur

  • Adverse reactions may require interventions such as decreasing the dose of TREANDA, or withholding or delaying treatment

  • TREANDA is contraindicated in patients with a known hypersensitivity to bendamustine or mannitol. Women should be advised to avoid becoming pregnant while using TREANDA

  • The most common non-hematologic adverse reactions associated with TREANDA (frequency ≥30%) were nausea, fatigue, vomiting, diarrhea, and pyrexia. The most common hematologic abnormalities associated with TREANDA (frequency ≥15%) were lymphopenia, leukopenia, anemia, neutropenia, and thrombocytopenia

TO REPORT SIDE EFFECTS: Contact us at 1-800-896-5855 or usmedinfo@cephalon.com

References
  1. Leoni LM, Bailey B, Reifert J, et al. Bendamustine (Treanda) displays a distinct pattern of cytotoxicity and unique mechanistic features compared with other alkylating agents. Clin Cancer Res. 2008;14:309-317.
  2. Strumberg D, Harstrick A, Doll K, Hoffmann B, Seeber S. Bendamustine hydrochloride activity against doxorubicin-resistant human breast carcinoma cell lines. Anticancer Drugs. 1996;7:415-421.
  3. Schwänen C, Hecker T, Hubinger G, et al. In vitro evaluation of bendamustine induced apoptosis in B-chronic lymphocytic leukemia. Leukemia. 2002;16:2096-2105.
  4. Goodman A. Bendamustine plus rituximab offers new standard of care for treatment of NHL and indolent lymphoma. Oncology NEWS International. 2010;19:1-3. http://www.cancernetwork.com/display/article/10165/1512720. Accessed April 12, 2011.
  5. Data on file. Cephalon, Inc.
Cephalon Oncology Financial Assistance
Reimbursement

Contact CORE: Cephalon Oncology Reimbursement Expertise for assistance and support

right arrow

right arrow

Download the Pivotal NHL Trial

Bendamustine is effective therapy in patients with rituximab-refractory, indolent B-cell NHL>>

This article contains information that may differ from the TREANDA Prescribing Information. Please review this article in conjunction with the accompanying full Prescribing Information.

right arrow


Get Adobe Flash player

You need Adobe Flash Player 9 or higher for the optimal viewing experience. Click on the button above to install the latest version of Adobe Flash Player 9.